ORPHA:2809
Familial recurrent peripheral facial palsy
Synonyms: Familial recurrent Bell palsy
- Type
- Disease
- Group
- Disorder
- Age of onset
- Adolescent, Adult, Childhood
- Status
- active
A rare peripheral neuropathy characterized by an acute onset of unilateral facial muscle weakness with Bell's phenomenon. It is non-progressive, resolves spontaneously, and it might be recurrent with no obvious precipitating factors.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Familial recurrent peripheral facial palsy | Familial recurrent Bell palsy |
| fr | Paralysie faciale périphérique récurrente familiale | Paralysie de Bell récurrente familiale |
| de | Fazialisparese, periphere rekurrente, familiäre Form | Gesichtslähmung, familiäre rekurrente |
| es | Parálisis facial periférica familiar recurrente | Parálisis familiar recurrente de Bell |
| it | Paralisi facciale periferica ricorrente familiare | |
| nl | Familiale recurrente perifere facialisparalyse | Familiale recurrente perifere aangezichtsverlamming van Bell |
| pt | Paralisia facial periférica recorrente familiar | Paralisia familiar recorrente de Bell |
| pl | Rodzinne nawracające obwodowe porażenie twarzy | Rodzinne nawracające porażenie twarzy Bella |
| cs | Familiární rekurentní periferní obrna | = en |
| uk | Сімейний рецидивуючий периферичний параліч обличчя | Сімейний рецидивуючий параліч Белла |
| zh | 家族性复发性外周性面瘫 | 家族性复发性贝尔麻痹 |
| tr | Ailesel tekrarlayan periferik yüz felci | Ailesel tekrarlayan Bell felci |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 134200 | E | validated | |
| ICD-10 | G51.0 | NTBT | attributed | validated |
| ICD-11 | 8B88.0 | NTBT | attributed | validated |
| MONDO | 0007592 | E | validated | |
| MeSH | C565028 | E | validated | |
| UMLS | C1851399 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98497Genetic peripheral neuropathy
rare genetic diseases; rare neurological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 100 000 | 5.6 / 100 000 | Worldwide | Value and class | Validated | 38435234[PMID]_ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2809
- This record as JSON: /data/d/2809.json